A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741920



Internal ID165586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109231122..109246795hg38UCSC Ensembl
chrX:108474351..108490024hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3815674
hg1915674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741920
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer